Canonical Allele Identifier: CA16620437

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 418068
• ClinVar RCV Id: RCV000480523 ; RCV000821444 ; RCV001016099
• dbSNP Id: rs1064793056

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092919_43092920delinsAC , CM000679.2:g.43092919_43092920delinsAC	GRCh38
NC_000017.10:g.41244936_41244937delinsAC , CM000679.1:g.41244936_41244937delinsAC	GRCh37
NC_000017.9:g.38498462_38498463delinsAC	NCBI36
NG_005905.2:g.125064_125065delinsGT , LRG_292:g.125064_125065delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2675_2676delinsGT
ENST00000461574.2:c.2611_2612delinsGT	ENSP00000417241.2:p.Pro871Val
ENST00000470026.6:c.2611_2612delinsGT	ENSP00000419274.2:p.Pro871Val
ENST00000473961.6:c.2485_2486delinsGT	ENSP00000420201.2:p.Pro829Val
ENST00000476777.6:c.2608_2609delinsGT	ENSP00000417554.2:p.Pro870Val
ENST00000477152.6:c.2533_2534delinsGT	ENSP00000419988.2:p.Pro845Val
ENST00000478531.6:c.784+1824_784+1825delinsGT	ENSP00000420412.2:n.784+1824_784+1825delinsGT
ENST00000489037.2:c.2533_2534delinsGT	ENSP00000420781.2:p.Pro845Val
ENST00000493919.6:c.646+1824_646+1825delinsGT	ENSP00000418819.2:n.646+1824_646+1825delinsGT
ENST00000494123.6:c.2611_2612delinsGT	ENSP00000419103.2:p.Pro871Val
ENST00000497488.2:c.1723_1724delinsGT	ENSP00000418986.2:p.Pro575Val
ENST00000618469.2:c.2611_2612delinsGT	ENSP00000478114.2:p.Pro871Val
ENST00000634433.2:c.2488_2489delinsGT	ENSP00000489431.2:p.Pro830Val
ENST00000644379.2:c.2611_2612delinsGT	ENSP00000496570.2:p.Pro871Val
ENST00000644555.2:c.646+1824_646+1825delinsGT	ENSP00000494614.2:n.646+1824_646+1825delinsGT
ENST00000652672.2:c.2470_2471delinsGT	ENSP00000498906.2:p.Pro824Val
ENST00000484087.6:c.664+1824_664+1825delinsGT	ENSP00000419481.2:n.664+1824_664+1825delinsGT
ENST00000700182.1:c.706+1824_706+1825delinsGT	ENSP00000514849.1:n.706+1824_706+1825delinsGT
ENST00000357654.9:c.2611_2612delinsGT MANE Select	ENSP00000350283.3:p.Pro871Val
ENST00000471181.7:c.2611_2612delinsGT	ENSP00000418960.2:p.Pro871Val
ENST00000352993.7:c.671-1888_671-1887delinsGT	ENSP00000312236.5:n.671-1888_671-1887delinsGT
ENST00000354071.7:c.2611_2612delinsGT	ENSP00000326002.7:p.Pro871Val
ENST00000357654.7:c.2611_2612delinsGT	ENSP00000350283.3:p.Pro871Val
ENST00000461221.5:c.*2394_*2395delinsGT	ENSP00000418548.1:n.*2394_*2395delinsGT
ENST00000468300.5:c.787+1824_787+1825delinsGT	ENSP00000417148.1:n.787+1824_787+1825delinsGT
ENST00000471181.6:c.2611_2612delinsGT	ENSP00000418960.2:p.Pro871Val
ENST00000478531.5:c.784+1824_784+1825delinsGT	ENSP00000420412.1:n.784+1824_784+1825delinsGT
ENST00000484087.5:c.409+1824_409+1825delinsGT	ENSP00000419481.1:n.409+1824_409+1825delinsGT
ENST00000487825.5:c.412+1824_412+1825delinsGT	ENSP00000418212.1:n.412+1824_412+1825delinsGT
ENST00000491747.6:c.787+1824_787+1825delinsGT	ENSP00000420705.2:n.787+1824_787+1825delinsGT
ENST00000493795.5:c.2470_2471delinsGT	ENSP00000418775.1:p.Pro824Val
ENST00000493919.5:c.646+1824_646+1825delinsGT	ENSP00000418819.1:n.646+1824_646+1825delinsGT
ENST00000586385.5:c.5-28969_5-28968delinsGT	ENSP00000465818.1:n.5-28969_5-28968delinsGT
ENST00000591534.5:c.-43-18399_-43-18398delinsGT	ENSP00000467329.1:n.-43-18399_-43-18398delinsGT
ENST00000591849.5:c.-99+32351_-99+32352delinsGT	ENSP00000465347.1:n.-99+32351_-99+32352delinsGT
NM_007294.3:c.2611_2612delinsGT , LRG_292t1:c.2611_2612delinsGT	NP_009225.1:p.Pro871Val
NM_007297.3:c.2470_2471delinsGT	NP_009228.2:p.Pro824Val
NM_007298.3:c.787+1824_787+1825delinsGT	NP_009229.2:n.787+1824_787+1825delinsGT
NM_007299.3:c.787+1824_787+1825delinsGT	NP_009230.2:n.787+1824_787+1825delinsGT
NM_007300.3:c.2611_2612delinsGT	NP_009231.2:p.Pro871Val
NR_027676.1:n.2747_2748delinsGT
NM_007294.4:c.2611_2612delinsGT MANE Select	NP_009225.1:p.Pro871Val
NM_007297.4:c.2470_2471delinsGT	NP_009228.2:p.Pro824Val
NM_007299.4:c.787+1824_787+1825delinsGT	NP_009230.2:n.787+1824_787+1825delinsGT
NM_007300.4:c.2611_2612delinsGT	NP_009231.2:p.Pro871Val
NR_027676.2:n.2788_2789delinsGT